Rapid evolution of α-gliadin gene family revealed by analyzing Gli-2 locus regions of wild emmer wheat

Naxin Huo, Tingting Zhu, Shengli Zhang, Toni Mohr, Ming Cheng Luo, Jong Yeol Lee, Assaf Distelfeld, Susan Altenbach, Yong Q. Gu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

α-Gliadins are a major group of gluten proteins in wheat flour that contribute to the end-use properties for food processing and contain major immunogenic epitopes that can cause serious health-related issues including celiac disease (CD). α-Gliadins are also the youngest group of gluten proteins and are encoded by a large gene family. The majority of the gene family members evolved independently in the A, B, and D genomes of different wheat species after their separation from a common ancestral species. To gain insights into the origin and evolution of these complex genes, the genomic regions of the Gli-2 loci encoding α-gliadins were characterized from the tetraploid wild emmer, a progenitor of hexaploid bread wheat that contributed the AABB genomes. Genomic sequences of Gli-2 locus regions for the wild emmer A and B genomes were first reconstructed using the genome sequence scaffolds along with optical genome maps. A total of 24 and 16 α-gliadin genes were identified for the A and B genome regions, respectively. α-Gliadin pseudogene frequencies of 86% for the A genome and 69% for the B genome were primarily caused by C to T substitutions in the highly abundant glutamine codons, resulting in the generation of premature stop codons. Comparison with the homologous regions from the hexaploid wheat cv. Chinese Spring indicated considerable sequence divergence of the two A genomes at the genomic level. In comparison, conserved regions between the two B genomes were identified that included α-gliadin pseudogenes containing shared nested TE insertions. Analyses of the genomic organization and phylogenetic tree reconstruction indicate that although orthologous gene pairs derived from speciation were present, large portions of α-gliadin genes were likely derived from differential gene duplications or deletions after the separation of the homologous wheat genomes ~ 0.5 MYA. The higher number of full-length intact α-gliadin genes in hexaploid wheat than that in wild emmer suggests that human selection through domestication might have an impact on α-gliadin evolution. Our study provides insights into the rapid and dynamic evolution of genomic regions harboring the α-gliadin genes in wheat.

Original languageEnglish
Pages (from-to)993-1005
Number of pages13
JournalFunctional and Integrative Genomics
Volume19
Issue number6
DOIs
StatePublished - 1 Nov 2019

Funding

FundersFunder number
US Department of Agriculture
USDA-Agricultural Research Service CRIS2030-21430-014
National Science FoundationIOS 1238231, RDA PJ013149
National Science Foundation
Directorate for Biological Sciences1238231
Directorate for Biological Sciences
National Natural Science Foundation of ChinaU1204315, 31571667
National Natural Science Foundation of China

    Keywords

    • Celiac disease
    • Gene duplication
    • Genome evolution
    • Phylogeny
    • Wheat gluten proteins
    • α-Gliadin gene family

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